Organic Matter Diagenesis in Acidic Mine Lakes

The significance of organic matter origin for carbon oxidation via sulfate and iron reduction in the sediments of three acid mine lakes is analyzed. Carbon reactivity was estimated by fitting first‐order expressions to measured rates. Carbon oxidation rates via sulfate and ferric iron reduction ranged from 3.4 to 4.7 mmol m^–2 d^–1 and resembled those reported for freshwater lakes. The estimated reaction constants increased from about 10^–3 a^–1 at the interface to the former mine grounds to 0.05 to 0.2 a^–1 at the current sediment‐water interface. Aquatic organic matter accounted for an estimated 45...75% of total carbon oxidation rates while it amounted only to about 5...14% of the total organic matter that had been deposited. The results of this study suggest that in highly acidic mine lakes the reactivity of the deposited organic matter can rapidly increase after flooding, enhancing carbon oxidation and internal neutralization rates in the sediments.     

Role of Methane Cycling in Organic Matter Turnover in Different Types of Lakes

The rates of microbiological processes in CH₄ cycling and organic matter destruction in the bottom sediment and water of different types of lakes in the Upper Volga basin and Baltic countries are determined. The rates of CH₄ removal from silts and the peculiarities of its distribution in water mass as a function of the lake productivity and the character of water mixing in it are studied. The role of processes in CH₄ cycling in destruction is shown to increase with increasing lake productivity.     

Organic Matter Transformation in the Conjugate Series of Surface Water in Northern Karelia

Water Resources - The composition of organic matter in the conjugated series of natural water (soil, bog, creek, and lake water) has been considered. The composition of aliphatic and aromatic...     

Acid Rain and Natural Organic Matter (NOM)

Twentyfive years of research on the effects of acid rain on rivers and lakes has, to a very small extent, documented changes in the nature and properties of natural organic matter (NOM). In Western Norway, a "whole-watershed-artificial-acidification-experiment" took place in the period 1988–1996. The goals of this long-term experiment were to study the role of NOM in acidification of surface water and the effects of acid precipitation on the quality and properties of NOM. In the HUMEX project (Humic Lake Acidification Experiment) one half of a lake and the corresponding catchment was artificially acidified with H₂SO₄ and NH₄NO₃ over a period of 5 years. The other half of the lake and catchment served as a control. In addition to monitoring of the general chemical composition of the water from the two lake halves, a number of other chemical and biological characteristics were studied. Here, we report the results related to changes in the nature and chemical properties of NOM. During the first few years of acidification, a significantly lower concentration of NOM was recorded in the acidified half of the catchment, compared with the control. However, statistical analyses of all data (covering a 2-years pre-treatment period and 5 years of treatment) related to the concentration of NOM (TOC, colour, and UV absorbance) did not suggest any significant effect on the quantity of NOM. This apparent discrepancy between the initial decrease in the concentration of NOM and no effect when the whole 5-years period is considered, may be due to the results of two different simultaneous processes. The results suggest that there first was a reduction of TOC and colour, as a consequence of the acidification, followed by an increase, perhaps owing to increased fertilisation (nitrogen) and in addition to a general temperature increase during the period. In addition, short-term studies of the aquatic surface microlayers, lipophilicity of the NOM, content of organic sulfur, and molecular size indicate differences in the quality of the NOM between the two lake halves, which could affect light absorption.     

Space and Time Variations of Organic Matter in Caspian Sea Water

Water Resources - The analysis of data on the space and time variations of the concentrations and element composition of organic matter dissolved in Caspian Sea water over 2010–2015 showed...     

Assessing Organic Carbon and Suspended Matter Runoff in the Yenisei Basin

The concentrations of organic matter that enters the aquatic environment in dissolved form, organic matter fractions adsorbed on suspended mineral particles, and the total concentration of suspended matter in the Yenisei water were studied using rapid optical methods. Spectral characteristics of light attenuation and absorption by river water and its filtrates were analyzed in summer. Total discharges of organic carbon and suspended matter by the river were evaluated.     

Metal Distribution in Different Size Fractions of Natural Organic Matter

In this paper, size‐exclusion chromatography (SEC) was used to determine the metal concentration in different size fractions of a bog lake water. Two methods were applied: (a) preparative SEC with off‐line metal concentration analysis and (b) direct coupling of an analytical SEC system on‐line with an inductively‐coupled plasma mass spectrometer (ICP‐MS). In the preparative SEC measurements, maximum concentrations were found for different metal ions in different size fractions of the natural organic matter (NOM). Normalization of metal concentrations to dissolved organic carbon concentration (DOC) yielded two maxima in the high and in the very low molecular‐weight fractions. Whereas good recoveries were found for Al, Fe, and Ni, only 40% were obtained for Pb. This indicates that Pb formed labile complexes with NOM, and hence could strongly interact with the column material. In the experiments with the analytical SEC‐ICP‐MS system, the same trends were observed, but with even lower recoveries than in the preparative system. Sample preconcentration and storage were also investigated with respect to decrease in metal concentration. During the ultrafiltration preconcentration step Al and Fe were removed only to a small extent, whereas about half of the initial Pb was lost. This indicates that Al and Fe were mainly bound to high molecular‐weight fractions of NOM. In contrast to that, Al and in particular Fe were removed from solution more than proportionally with respect to DOC because of aggregation of the NOM during storage, whereas Pb and Ni were concentrated relative to the DOC.     

Organic Matter Utilization and Destruction in Water Bodies at Different Trophic Level

It has been established that phytoplankton actively takes up low-molecular organic compounds, while high-molecular organic matter is utilized mainly by bacterioplankton. It has been found that algae utilize high-molecular compounds only in the presence of bacteria, because the latter take up final products of hydrolysis rather than release lytic enzymes into the environment.     

Salinity and Soluble Organic Matter on Virus Sorption in Sand and Soil Columns

The objective of this research was to study the sorption and transport of bacteriophage MS-2 (a bacterial virus) in saturated sediments under the effect of salinity and soluble organic matter (SOM). One-dimensional column experiments were conducted on washed high-purity silica sand and sandy soil. In sand column tests, increasing salinity showed distinct effect on enhancing MS-2 sorption. However, SOM decreased MS-2 sorption. Using a two-site reversible-irreversible sorption model and the double layer theory, we explained that pore-water salinity potentially compressed the theoretical thickness of double layers of MS-2 and sand, and thus increased sorption on reversible sorption sites. On irreversible sorption sites, increasing salinity reversed charges of some sand particles from negative to positive, and thus converted reversible sorption sites into irreversible sites and enhanced sorption of MS-2. SOM was able to expand the double layer thickness on reversible sites and competed with MS-2 for the same binding place on irreversible sites. In sandy soil column tests, the bonded and dissolved (natural) soil organic matters suppressed the effects of pore-water salinity and added SOM and significantly reduced MS-2 adsorption. This was explained that the bonded soil organic matter occupied a great portion of sorption sites and significantly reduced sorption sites for MS-2. In addition, the dissolved soil organic matter potentially expanded the double layer thickness of MS-2 and sandy soil on reversible sorption sites and competed with MS-2 for the same binding place.     

太湖湖区有机物流失模拟

研究了１９９２－１９９４年女山湖大面积围栏养蟹利用与保护沉水植物资源的效果结果表明：围栏内河蟹的食物组成中,主要有菹草、苦草、金鱼藻、马来眼子菜、黄丝草和黑藻等沉水植物．其中菹草、黑藻的出现频率和概念生物量,分别在４、６、７、８和９月为最高;围栏内沉水植物的种类和生物量的变化与河蟹的放养密度关系密切,当河蟹的放养密度不超过３０只·ｈｍ~（－２）时,围栏内沉水植物的生物量与对照组均有明显的增加趋势,由此可证,女山湖大面积的围栏养蟹和适宜的放养密度,有效地利用和保护了围栏区内的沉水植物资源     

沉积物中有机质的环境行为研究进展

水体沉积物是重金属,有毒有机化合物等环境污染物及C,N,P等营养元素的汇和释放源,而有机质对灾些污染物和营养元素在沉积物中的迁移,转化等地球化学行为中起着至关重要的作用,本文就近期有关沉积物中有机质的环境地球化学行为为方面的研究进行了综述,重点评述了有关沉积物中有机质本身的来源,性质,迁移和矿化及其环境效应等方面的研究进展。     

Carbon Budget and Molecular Structure of Natural Organic Matter in Bank Infiltrated Groundwater

Managed aquifer recharge (MAR) provides means to remove natural organic matter (NOM) from surface waters. Recent studies have explored the degree of NOM removal in groundwater. In this study, we further elaborate the NOM removal at a lakeside natural bank infiltration site that functions as a surrogate for MAR. Our objective was to quantify the carbon budget in the aquifer based on concentration measurements of dissolved (in)organic carbon, and the molecular changes in NOM using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). According to the carbon budget, only 25% of the dissolved carbon entering the aquifer was organic, and it predominantly originated from lake water. Of the inorganic majority, on average 40% was produced in the vadose zone above the groundwater table, 31% in the lake bank, 22% in the aquifer as a result of degrading organic matter of lake water, and 7% in the lake. Seasonal concentration variations suggested that the lake bank was the main carbon source in the summer, increasing the carbon concentration of infiltrating lake water, that is, 3.0 mg/L to 7.9 mg/L. FT-ICR MS results showed 4960 to 5330 individual compounds in lake and groundwater. NOM removal in the aquifer was selective: the relative abundance of oxygen-containing species decreased from 75 to 31%, while the relative abundance of sulfur-containing species increased from 15 to 57%. The average molecular weights of both species remained unchanged. The study highlighted the role of lake bank processes and sulfur-containing species in groundwater quality.     

Earthquake distribution and volcanism in Kamchatka,Kurile Islands,and Hokkaido Part 1: Kamchatka and northern Kuriles

Summary The morphology of the Wadati-Benioff zone in the region of Kamchatka and Northern Kuriles, based on the distribution of 1102 earthquake foci, verified the existence of an intermediate depth aseismic gap and its relation to active andesitic volcanism. A system of deep seismically active fracture zones, genetically connected with the process of subduction, was delineated in the continental plate and confirmed by the results of deep seismic sounding. Two of these fractures, dipping toward the subduction zone, may be considered as the principal feeding channels for active and Holocene volcanoes of the continental volcanic belts of Kamchatka.     

Effect of a Flood in the Amur River on Organic Matter Dynamics in Groundwater

The space and time dynamics of organic matter concentration in groundwater in the Tungusskoe deposit during the historical 2013 flood in the Amur River is discussed. For comparison analysis, several methods for determining the quantitative characteristics of organic matter (spectrophotometry, gas-chromatographic mass spectrometry, and high-performance liquid chromatography) were applied to different layers of an aquifer at different distances from the shore line. The genesis of many organic substances is due to the inflow of river filtrate and surface water from the inundated floodplain. In the post-flood 2014, groundwater showed a decrease in the total amount of organic components and the presence of low-molecular hydrocarbons, diphenylamine, cosanes, phenanthrene, naphthalene, and derivatives of stearic and palmitic acids. Toxic methyl benzene was identified in most wells.     

Examining the Extraction Efficiency of Petroleum-Derived Dissolved Organic Matter in Contaminated Groundwater Plumes

The extraction efficiency of petroleum-derived dissolved organic matter (DOM) was examined for groundwater samples from an aquifer contaminated with crude oil. Five different types of extraction techniques were investigated to determine which method is best suited for the analysis of potentially toxic petroleum-derived DOM. The five types were a liquid-liquid extraction (LLE) with dichloromethane (DCM) and total petroleum hydrocarbons-diesel range (TPH_d) with DCM (EPA method 3510C), and three solid-phase extraction (SPE) stationary phases that are routinely used for extraction of polar analytes from water. For the LLE and TPH_d, that is selective for nonpolar compounds, the extraction efficiency of petroleum-derived DOM decreased downgradient as the petroleum-derived DOM becomes increasingly polar due to biodegradation. In contrast, the average extraction efficiency by the SPE methods was greater than 65% across the gradient. The results showed that SPE is more efficient for extracting petroleum-derived DOM at hydrocarbon-contaminated sites. The use of a method with greater extraction efficiency for partially oxidized hydrocarbons may prove useful in determining relationships between their composition and structure and potential for risks to human health or the environment.